Canonical Allele Identifier: CA1429666100

Gene: FGF12

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.192335434C= , CM000665.2:g.192335434C=	GRCh38
NC_000003.11:g.192053223C= , CM000665.1:g.192053223C=	GRCh37
NC_000003.10:g.193535917C=	NCBI36
NG_051966.1:g.397166G=

Transcript Alleles

HGVS	Amino-acid Change
NM_004113.6:c.155G= MANE Select	NP_004104.3:p.Arg52=
ENST00000445105.7:c.155G= MANE Select	ENSP00000393686.1:p.Arg52=
NM_001377292.1:c.44G=	NP_001364221.1:p.Arg15=
NM_001377293.1:c.83G=	NP_001364222.1:p.Arg28=
NM_001377294.1:c.83G=	NP_001364223.1:p.Arg28=
NM_004113.5:c.155G=	NP_004104.3:p.Arg52=
NM_021032.4:c.341G=	NP_066360.1:p.Arg114=
NM_021032.5:c.341G=	NP_066360.1:p.Arg114=
ENST00000418610.1:c.155G=	ENSP00000395517.1:p.Arg52=
ENST00000430714.5:c.44G=	ENSP00000410125.1:p.Arg15=
ENST00000445105.6:c.155G=	ENSP00000393686.1:p.Arg52=
ENST00000448795.5:c.83G=	ENSP00000412904.1:p.Arg28=
ENST00000450716.5:c.155G=	ENSP00000397635.1:p.Arg52=
ENST00000454309.6:c.341G=	ENSP00000413496.2:p.Arg114=
ENST00000454309.7:c.341G=	ENSP00000413496.2:p.Arg114=
ENST00000682572.1:n.343G=
ENST00000682819.1:n.374G=
ENST00000682819.2:n.408G=
ENST00000683451.1:c.155G=	ENSP00000508366.1:p.Arg52=
ENST00000683451.2:c.155G=	ENSP00000508366.1:p.Arg52=
ENST00000683935.1:c.155G=	ENSP00000507098.1:p.Arg52=
ENST00000684282.1:c.83G=	ENSP00000507149.1:p.Arg28=
ENST00000684728.1:c.83G=	ENSP00000506839.1:p.Arg28=
XM_005247227.1:c.233G=	XP_005247284.1:p.Arg78=
XM_005247227.2:c.233G=	XP_005247284.1:p.Arg78=
XM_006713538.2:c.146G=	XP_006713601.1:p.Arg49=
XM_006713538.3:c.146G=	XP_006713601.1:p.Arg49=
XM_006713539.2:c.83G=	XP_006713602.1:p.Arg28=
XM_024453395.1:c.83G=	XP_024309163.1:p.Arg28=